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FDA 510(k)

ACL TOP 700 LAS

K-Number: K091980 · 2009-09-22

Decision Date2009-09-22
Product CodeGKP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ACL TOP 700 LAS is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 2009-09-22 under 510(k) number K091980. The device is classified under product code GKP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACL TOP 700 LAS?

ACL TOP 700 LAS is a medical device that received FDA 510(k) clearance on 2009-09-22. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K091980.

When did ACL TOP 700 LAS receive FDA 510(k) clearance?

ACL TOP 700 LAS received FDA 510(k) clearance on 2009-09-22, under 510(k) number K091980.

Who is the listed applicant for ACL TOP 700 LAS?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACL TOP 700 LAS?

The FDA product code for ACL TOP 700 LAS is GKP.

Other records listing Instrumentation Laboratory CO as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 315 devices →

Related Devices (Code: GKP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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